Target deconvolution is a vital initial step in preclinical drug development to determine research focus and strategy. In this respect, computational target prediction is used to identify the most probable targets of an orphan ligand or the most similar targets to a protein under investigation. Applications range from the fundamental analysis of the mode-of-action over polypharmacology or adverse effect predictions to drug repositioning. Here, we provide a review on published ligand- and target-based as well as hybrid approaches for computational target prediction, together with current limitations and future directions.

The analysis on tool imbalance, backed by the empirical results, indicates the need and superiority of the proposed framework over state-of-the-art techniques.

This study's objective was the generation of a standardized geometry of the healthy nasal cavity. An average geometry of the healthy nasal cavity was generated using a statistical shape model based on 25 symptom-free subjects. Airflow within the average geometry and these geometries was calculated using fluid simulations. Integral measures of the nasal resistance, wall shear stresses (WSS) and velocities were calculated as well as cross-sectional areas (CSA). Furthermore, individual WSS and static pressure distributions were mapped onto the average geometry. The average geometry featured an overall more regular shape that resulted in less resistance, reduced WSS and velocities compared to the median of the 25 geometries. Spatial distributions of WSS and pressure of the average geometry agreed well compared to the average distributions of all individual geometries. The minimal CSA of the average geometry was larger than the median of all individual geometries (83.4 vs. 74.7 mm²). The airflow observed within the average geometry of the healthy nasal cavity did not equal the average airflow of the individual geometries. While differences observed for integral measures were notable, the calculated values for the average geometry lay within the distributions of the individual parameters. Spatially resolved parameters differed less prominently.The nose is the main passageway for respired air to flow from ambient to the lungs and vice versa. Air flowing through the nose is humidified, tempered and cleansed from particles, which could harm the intricate structures of the lungs. While the anatomy of the nose can easily be investigated from the outside using either a speculum or an endoscope, the nature of healthy nasal airflow is not yet fully understood. Nonetheless, there were extensive efforts as well as remarkable progress to better understand the complex airflow within the nose.While investigation of the airflow within the nasal cavity began with in-vitro experiments using either cadaver castings or upscaled models 1-3 , numerical simulation of nasal airflow became the quasi standard within the last decade and is now widely used 4-6 . Here, the patient-specific geometry of the nasal cavity is reconstructed using computed tomography (CT) scans.Recently, first studies were able to reveal correlations between numerically calculated flow parameters and the perceived nasal patency of a patient. Zhao et al. were able to show, that a significant correlation between cooling of the mucosal layer, a process that is associated with trigeminal function, is correlated with patency ratings of the nose 7,8 . In more recent studies, they were able to reveal differences in wall shear stress and heat flux between symptomatic and asymptomatic patients with septal perforations 9 and they were also able to show, that numerical simulations might help to understand complex relationships between surgical procedures and the development of empty nose syndrome 10 . Sanmiguel-Rojas et al. proposed another approach, where two non-dimensional par...

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Alpha-solenoids are flexible protein structural domains formed by ensembles of alpha-helical repeats (Armadillo and HEAT repeats among others). While homology can be used to detect many of these repeats, some alpha-solenoids have very little sequence homology to proteins of known structure and we expect that many remain undetected. We previously developed a method for detection of alpha-helical repeats based on a neural network trained on a dataset of protein structures. Here we improved the detection algorithm and updated the training dataset using recently solved structures of alpha-solenoids. Unexpectedly, we identified occurrences of alpha-solenoids in solved protein structures that escaped attention, for example within the core of the catalytic subunit of PI3KC. Our results expand the current set of known alpha-solenoids. Application of our tool to the protein universe allowed us to detect their significant enrichment in proteins interacting with many proteins, confirming that alpha-solenoids are generally involved in protein-protein interactions. We then studied the taxonomic distribution of alpha-solenoids to discuss an evolutionary scenario for the emergence of this type of domain, speculating that alpha-solenoids have emerged in multiple taxa in independent events by convergent evolution. We observe a higher rate of alpha-solenoids in eukaryotic genomes and in some prokaryotic families, such as Cyanobacteria and Planctomycetes, which could be associated to increased cellular complexity. The method is available at http://cbdm.mdc-berlin.de/~ard2/.